X-linked cone-rod dystrophy 3
cone-rod dystrophy that has material basis in mutation in the CACNA1F gene on chromosome Xp11
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X-linked cone-rod dystrophy 3
Summary
X-linked cone-rod dystrophy 3 is a rare disease[1].
Key Facts
- X-linked cone-rod dystrophy 3's instance of is recorded as rare disease[2].
- X-linked cone-rod dystrophy 3's instance of is recorded as class of disease[3].
- X-linked cone-rod dystrophy 3's subclass of is recorded as cone-rod dystrophy[4].
- X-linked cone-rod dystrophy 3's subclass of is recorded as X-linked recessive disease[5].
- X-linked cone-rod dystrophy 3's MeSH descriptor ID is recorded as C564507[6].
- X-linked cone-rod dystrophy 3's OMIM ID is recorded as 300476[7].
- X-linked cone-rod dystrophy 3's Disease Ontology ID is recorded as DOID:0111007[8].
- X-linked cone-rod dystrophy 3's genetic association is recorded as CACNA1F[9].
- X-linked cone-rod dystrophy 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111007[10].
- X-linked cone-rod dystrophy 3's exact match is recorded as http://identifiers.org/doid/DOID:0111007[11].
- X-linked cone-rod dystrophy 3's UMLS CUI is recorded as C1845407[12].
- X-linked cone-rod dystrophy 3's GARD rare disease ID is recorded as 10654[13].
- X-linked cone-rod dystrophy 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- X-linked cone-rod dystrophy 3's Mondo ID is recorded as MONDO_0010335[15].
- X-linked cone-rod dystrophy 3's UniProt disease ID is recorded as DI-00328[16].